A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578799



Internal ID16019522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19790327..19857161hg38UCSC Ensembl
Innerchr19:19901136..19967970hg19UCSC Ensembl
Innerchr19:19762136..19828970hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3866835
hg1966835
hg1866835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896157
Samples
Known GenesZNF506
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578799
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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